Classifications

• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
  • G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
  • G02B1/041—Lenses
  • G02B1/043—Contact lenses
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
  • A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
  • A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
  • A61L27/52—Hydrogels or hydrocolloids

Definitions

• the present invention generally relates to biomedical devices such as ophthalmic lenses.
• Biomedical devices such as contact lenses are made of various polymeric materials, including rigid gas permeable materials, soft elastomeric materials, and soft hydrogel materials.
• the majority of contact lenses sold today are made of soft hydrogel materials.
• Hydrogels are a cross-linked polymeric system that absorb and retain water, typically 10 to 80 percent by weight, and especially 20 to 70 percent water.
• Hydrogel lenses are commonly prepared by polymerizing a lens-forming monomer mixture including at least one hydrophilic monomer, such as 2-hydroxyethyl methacrylate, N,N-dimethylacrylamide, N-vinyl-2-pyrrolidone, glycerol methacrylate, and methacrylic acid.
• silicone hydrogel lenses In the case of silicone hydrogel lenses, a silicone-containing monomer is copolymerized with the hydrophilic monomers. Regardless of their water content, both hydrogel and non-hydrogel siloxy and/or fluorinated contact lenses tend to have relatively hydrophobic, non-wettable surfaces.
• silicone lenses One problem associated with silicone lenses is the surfacing of silicone chains which create hydrophobic areas on the lens. This will adversely impact wettability, on eye-movement and comfort to the user.
• biomedical devices such as contact lenses that exhibit suitable physical and chemical properties, e.g., oxygen permeability, lubriciousness and wettability, for prolonged contact with the body while also being biocompatible. It would also be desirable to provide improved biomedical devices that are easy to manufacture in a simple, cost effective manner.
• a biomedical device comprising a polymerization product of a mixture comprising (a) a hydrophilic polymer comprising hydrophilic units and one or more thio carbonyl thio fragments of a reversible addition fragmentation chain transfer (“RAFT”) agent; and (b) one or more biomedical device-forming monomers.
• RAFT reversible addition fragmentation chain transfer
• an ophthalmic lens comprising a polymerization product of a mixture comprising (a) a hydrophilic polymer comprising hydrophilic units and one or more thio carbonyl thio fragments of a RAFT agent; and (b) one or more ophthalmic lens-forming monomers.
• the biomedical devices of the present invention are advantageously formed from hydrophilic polymers containing one or more hydrophilic units and one or more thio carbonyl thio fragments of a RAFT agent.
• the hydrophilic polymers containing one or more hydrophilic units and one or more thio carbonyl thio fragments of a RAFT agent are non-amphophilic polymers and are capable of forming biomedical devices with a hydrophilic or lubricious (or both) surface.
• Hydrophilic and/or lubricious surfaces of the biomedical devices herein such as contact lenses substantially prevent or limit the adsorption of tear lipids and proteins on, and their eventual absorption into, the lenses, thus preserving the clarity of the contact lenses. This, in turn, preserves their performance quality thereby providing a higher level of comfort to the wearer.
• biomedical devices intended for direct contact with body tissue or body fluid.
• a “biomedical device” is any article that is designed to be used while either in or on mammalian tissues or fluid, and preferably in or on human tissue or fluids.
• Representative examples of biomedical devices include, but are not limited to, artificial ureters, diaphragms, intrauterine devices, heart valves, catheters, denture liners, prosthetic devices, ophthalmic lens applications, where the lens is intended for direct placement in or on the eye, such as, for example, intraocular devices and contact lenses.
• the preferred biomedical devices are ophthalmic devices, particularly contact lenses, and most particularly contact lenses made from hydrogels.
• ophthalmic device refers to devices that reside in or on the eye. These devices can provide optical correction, wound care, drug delivery, diagnostic functionality or cosmetic enhancement or effect or a combination of these properties.
• Useful ophthalmic devices include, but are not limited to, ophthalmic lenses such as soft contact lenses, e.g., a soft, hydrogel lens, soft, non-hydrogel lens and the like, hard contact lenses, e.g., a hard, gas permeable lens material and the like, intraocular lenses, overlay lenses, ocular inserts, optical inserts and the like.
• a lens is considered to be “soft” if it can be folded back upon itself without breaking.
• the biomedical devices of the present invention are formed from a polymerization product of a mixture comprising (a) a hydrophilic polymer comprising one or more hydrophilic units and one or more thio carbonyl thio fragments of a reversible addition fragmentation chain transfer (“RAFT”) agent; and (b) one or more biomedical device-forming monomers.
• RAFT reversible addition fragmentation chain transfer
• the term “hydrophilic polymers” as used herein shall be understood to mean a hydrophilic polymer containing polar or charged functional groups rendering it water-soluble.
• Hydrophilic polymers comprising one or more hydrophilic units and one or more thio carbonyl thio fragments of a RAFT agent are prepared via RAFT polymerization, i.e., monomers are polymerized via a RAFT mechanism to form the hydrophilic polymer, e.g., a block or random copolymer in which the molecular weight of each of the blocks and the entire polymer can be precisely controlled.
• RAFT polymerization is a radical polymerization technique that enables polymers to be prepared having a well defined molecular architecture and low polydispersity.
• the RAFT agents suitable for use herein are based upon thio carbonyl thio chemistry which is well known to those of ordinary skill in the art.
• the RAFT agent can be, for example, a xanthate-containing compound, trithiocarbonate-containing compound, dithiocarbamate-containing compound or dithio ester-containing compound, wherein each compound contains a thiocarbonyl thio group.
• One class of RAFT agents that can be used herein is of the general formula:
• Z is a substituted oxygen (e.g., xanthates (—O—R)), a substituted nitrogen (e.g., dithiocarbamates (—NRR)), a substituted sulfur (e.g., trithiocarbonates (—S—R)), a substituted or unsubstituted C 1 -C 20 alkyl or C 3 -C 25 unsaturated, or partially or fully saturated ring (e.g., dithioesters (—R)) or a carboxylic acid-containing group; and R is independently a straight or branched, substituted or unsubstituted C 1 -C 30 alkyl group, a substituted or unsubstituted C 3 -C 30 cycloalkyl group, a substituted or unsubstituted C 3 -C 30 cycloalkylalkyl group, a substituted or unsubstituted C 3 -C 30 cycloalkenyl group
• alkyl groups for use herein include, by way of example, a straight or branched alkyl chain radical containing carbon and hydrogen atoms of from 1 to about 30 carbon atoms and preferably from 1 to about 12 carbon atoms with or without unsaturation, to the rest of the molecule, e.g., methyl, ethyl, n-propyl, 1-methylethyl (isopropyl), n-butyl, n-pentyl, methylene, ethylene, etc., and the like.
• a straight or branched alkyl chain radical containing carbon and hydrogen atoms of from 1 to about 30 carbon atoms and preferably from 1 to about 12 carbon atoms with or without unsaturation, to the rest of the molecule e.g., methyl, ethyl, n-propyl, 1-methylethyl (isopropyl), n-butyl, n-pentyl, methylene, ethylene, etc.,
• cycloalkyl groups for use herein include, by way of example, a substituted or unsubstituted non-aromatic mono or multicyclic ring system of about 3 to about 30 carbon atoms and preferably from 3 to about 6 carbon atoms such as, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, perhydronapththyl, adamantyl and norbornyl groups, bridged cyclic groups or sprirobicyclic groups, e.g., spiro-(4,4)-non-2-yl and the like, optionally containing one or more heteroatoms, e.g., O and N, and the like.
• cycloalkylalkyl groups for use herein include, by way of example, a substituted or unsubstituted cyclic ring-containing radical containing from about 3 to about 30 carbon atoms and preferably from 3 to about 6 carbon atoms directly attached to the alkyl group which are then attached to the main structure of the monomer at any carbon from the alkyl group that results in the creation of a stable structure such as, for example, cyclopropylmethyl, cyclobutylethyl, cyclopentylethyl and the like, wherein the cyclic ring can optionally contain one or more heteroatoms, e.g., O and N, and the like.
• a substituted or unsubstituted cyclic ring-containing radical containing from about 3 to about 30 carbon atoms and preferably from 3 to about 6 carbon atoms directly attached to the alkyl group which are then attached to the main structure of the monomer at any carbon from the alkyl group that results in the creation of
• cycloalkenyl groups for use herein include, by way of example, a substituted or unsubstituted cyclic ring-containing radical containing from about 3 to about 30 carbon atoms and preferably from 3 to about 6 carbon atoms with at least one carbon-carbon double bond such as, for example, cyclopropenyl, cyclobutenyl, cyclopentenyl and the like, wherein the cyclic ring can optionally contain one or more heteroatoms, e.g., O and N, and the like.
• aryl groups for use herein include, by way of example, a substituted or unsubstituted monoaromatic or polyaromatic radical containing from about 5 to about 30 carbon atoms such as, for example, phenyl, naphthyl, tetrahydronapthyl, indenyl, biphenyl and the like, optionally containing one or more heteroatoms, e.g., O and N, and the like.
• arylalkyl groups for use herein include, by way of example, a substituted or unsubstituted aryl group as defined herein directly bonded to an alkyl group as defined herein, e.g., —CH 2 C 6 H 5 , —C 2 H 5 C 6 H 5 and the like, wherein the aryl group can optionally contain one or more heteroatoms, e.g., O and N, and the like.
• ester groups for use herein include, by way of example, a carboxylic acid ester having one to 20 carbon atoms and the like.
• ether or polyether containing groups for use herein include, by way of example, an alkyl ether, cycloalkyl ether, cycloalkylalkyl ether, cycloalkenyl ether, aryl ether, arylalkyl ether wherein the alkyl, cycloalkyl, cycloalkylalkyl, cycloalkenyl, aryl, and arylalkyl groups are as defined herein.
• ether or polyether-containing groups include, by way of example, alkylene oxides, poly(alkylene oxide)s such as ethylene oxide, propylene oxide, butylene oxide, poly(ethylene oxide)s, poly(ethylene glycol)s, poly(propylene oxide)s, poly(butylene oxide)s and mixtures or copolymers thereof, an ether or polyether group of the general formula —(R 2 OR 3 ) t , wherein R 2 is a bond, a substituted or unsubstituted alkyl, cycloalkyl or aryl group as defined herein and R 3 is a substituted or unsubstituted alkyl, cycloalkyl or aryl group as defined herein and t is at least 1, e.g., —CH 2 CH 2 OC 6 H 5 and CH 2 —CH 2 —CH 2 —O—CH 2 —(CF 2 ) z H where z is 1 to 6, —CH 2 CH 2 OC 2 H 5
• alkyl or arylamide groups for use herein include, by way of example, an amide of the general formula —R 4 C(O)NR 5 R 6 wherein R 4 , R 5 and R 6 are independently C 1 -C 30 hydrocarbons, e.g., R 4 can be alkylene groups, arylene groups, cycloalkylene groups and R 5 and R 6 can be alkyl groups, aryl groups, and cycloalkyl groups as defined herein and the like.
• alky or arylamine groups for use herein include, by way of example, an amine of the general formula —R 7 NR 8 R 9 wherein R 7 is a C 2 -C 30 alkylene, arylene, or cycloalkylene and R 8 and R 9 are independently C 1 -C 30 hydrocarbons such as, for example, alkyl groups, aryl groups, or cycloalkyl groups as defined herein.
• heterocyclic ring groups for use herein include, by way of example, a substituted or unsubstituted stable 3 to about 30 membered ring radical, containing carbon atoms and from one to five heteroatoms, e.g., nitrogen, phosphorus, oxygen, sulfur and mixtures thereof.
• Suitable heterocyclic ring radicals for use herein may be a monocyclic, bicyclic or tricyclic ring system, which may include fused, bridged or spiro ring systems, and the nitrogen, phosphorus, carbon, oxygen or sulfur atoms in the heterocyclic ring radical may be optionally oxidized to various oxidation states.
• the nitrogen atom may be optionally quaternized; and the ring radical may be partially or fully saturated (i.e., heteroaromatic or heteroaryl aromatic).
• heterocyclic ring radicals include, but are not limited to, azetidinyl, acridinyl, benzodioxolyl, benzodioxanyl, benzofurnyl, carbazolyl, cinnolinyl, dioxolanyl, indolizinyl, naphthyridinyl, perhydroazepinyl, phenazinyl, phenothiazinyl, phenoxazinyl, phthalazinyl, pyridyl, pteridinyl, purinyl, quinazolinyl, quinoxalinyl, quinolinyl, isoquinolinyl, tetrazoyl, imidazolyl, tetrahydroquinoliny
• heteroaryl groups for use herein include, by way of example, a substituted or unsubstituted heterocyclic ring radical as defined herein.
• the heteroaryl ring radical may be attached to the main structure at any heteroatom or carbon atom that results in the creation of a stable structure.
• heteroarylalkyl groups for use herein include, by way of example, a substituted or unsubstituted heteroaryl ring radical as defined herein directly bonded to an alkyl group as defined herein.
• the heteroarylalkyl radical may be attached to the main structure at any carbon atom from the alkyl group that results in the creation of a stable structure.
• heterocyclic groups for use herein include, by way of example, a substituted or unsubstituted heterocylic ring radical as defined herein.
• the heterocyclic ring radical may be attached to the main structure at any heteroatom or carbon atom that results in the creation of a stable structure.
• heterocycloalkyl groups for use herein include, by way of example, a substituted or unsubstituted heterocylic ring radical as defined herein directly bonded to an alkyl group as defined herein.
• the heterocycloalkyl radical may be attached to the main structure at any carbon atom in the alkyl group that results in the creation of a stable structure.
• the substituents in the ‘substituted oxygen’, ‘substituted nitrogen’, ‘substituted sulfur’, ‘substituted alkyl’, ‘substituted alkylene, ‘substituted cycloalkyl’, ‘substituted cycloalkylalkyl’, ‘substituted cycloalkenyl’, ‘substituted arylalkyl’, ‘substituted aryl’, ‘substituted heterocyclic ring’, ‘substituted heteroaryl ring,’ substituted heteroarylalkyl', ‘substituted heterocycloalkyl ring’, ‘substituted cyclic ring’ may be the same or different and include one or more substituents such as hydrogen, hydroxy, halogen, carboxyl, cyano, nitro, oxo ( ⁇ O), thio( ⁇ S), substituted or unsubstituted alkyl, substitute
• x is 2 and R is an ether or polyether containing group as defined above.
• the RAFT agent can be prepared according to the following general scheme:
• RAFT agents Another class of RAFT agents that can be used herein is of the general formula:
• x and Z have the aforestated meanings and R 10 is a substituted or unsubstituted carboxylic acid-containing group.
• a carboxylic acid-containing group for use herein include, by way of example, a carboxylic acid group attached to the rest of the molecule via a linking group, e.g., of the general formula —R 11 C(O)OH, wherein R 11 is a bond, a substituted or unsubstituted alkylene group, a substituted or unsubstituted cycloalkylene group, a substituted or unsubstituted cycloalkylalkylene group, a substituted or unsubstituted arylene or a substituted or unsubstituted arylalkylene group as defined herein, e.g., —CH(Ar)(C(O)OH), —C(CH 3 )(C(O)OH), and the like, wherein the carboxylic acid group can be attached to the substituent or attached directly to alkylene group, cycloalkylene group, cycloalkylalkylene group, arylene or
• RAFT agents for use herein include, but are not limited to, benzyl dodecyl trithiocarbonate, ethyl-2-dodecyl trithiocarbony) proprionate, S-sec propionic acid O-ethyl xanthate, ⁇ -ethyl xanthylphenylacetic acid, ethyl ⁇ -(o-ethyl xanthyl) proprionate, ethyl ⁇ -(ethyl xanthyl)phenyl acetate, ethyl 2-(dodecyl trithiocarbonyl)phenyl acetate, ethyl 2-(dodecyl trithiocarbonyl) propionate, 2-(dodecylthiocarbonylthiol)propanoic acid, and the like and mixtures thereof.
• RAFT agent there is no particular limitation on the organic chemistry used to form the RAFT agent and is within the purview of one skilled in the art. Also, the working examples below provide guidance.
• the RAFT agents can be prepared as exemplified in Schemes I-III below.
• the hydrophilic polymers described herein also contain one or more hydrophilic units.
• the hydrophilic unit(s) is derived from at least one hydrophilic monomer.
• Suitable hydrophilic monomer include, by way of example, acrylamides such as N,N-dimethylacrylamide, N,N-dimethylmethacrylamide, and the like; acetamides such as N-vinyl-N-methyl acetamide, N-vinyl acetamide and the like; formamides such as N-vinyl-N-methyl formamide, N-vinyl formamide, and the like; cyclic lactams such as N-vinyl-2-pyrrolidone and the like; (meth)acrylated alcohols such as 2-hydroxyethyl methacrylate, 2-hydroxyethyl acrylate and the like; (meth)acrylated poly(ethyleneglycol)s and the like; ethylenically unsaturated carboxylic acids such as methacrylic acid, acrylic acid and the like and mixtures thereof.
• acrylamides such as N,N-dimethylacrylamide, N,N-dimethylmethacrylamide, and the like
• the hydrophilic polymers containing one or more thio carbonyl thio fragments of a RAFT agent can also include a hydrophilic unit derived from an ethylenically unsaturated polymerizable monomer having ring-opening reactive functionalities.
• Such monomers may include one or more ring-opening reactive groups such as, for example, azlactone, epoxy, acid anhydrides, and the like.
• Suitable polymerizable monomer having ring-opening reactive functionalities include, but are not limited to, glycidyl methacrylate (GMA), maleic anhydride, itaconic anhydride and the like and mixtures thereof.
• the units derived from an ethylenically unsaturated polymerizable monomer having ring-opening reactive functionalities can be copolymerized with a hydrophilic comonomer to form the hydrophilic units in the resulting hydrophilic polymers.
• comonomers useful to be copolymerized with the ring-opening reactive functionalities of the monomer to form hydrophilic polymers used to prepare a biomedical device include those mentioned above, with dimethylacrylamide, hydroxyethyl methacrylate (HEMA), and/or N-vinylpyrrolidone being preferred.
• the unit derived from the ethylenically unsaturated polymerizable hydrophilic monomers having ring-opening reactive functionalities can be subjected to a ring-opening reaction, e.g., by hydrolyzing with water, and form hydrophilic units in the resulting hydrophilic polymer.
• the hydrophilic polymers containing one or more thio carbonyl thio fragments of a RAFT agent can also include a unit derived from an ethylenically unsaturated polymerizable alkoxylated polymer.
• Suitable ethylenically unsaturated polymerizable alkoxylated polymers include, by way of example, polymerizable polyethylene glycols having a molecular weight of up to, for example, about 1000 such as those with CTFA names PEG-200, PEG-400, PEG-600, PEG-1000, and mixtures thereof.
• Representative examples include PEG-200 methacrylate, PEG-400 methacrylate, PEG-600 methacrylate, PEG-1000 methacrylate and the like and mixtures thereof.
• the size of the units derived from an ethylenically unsaturated polymerizable alkoxylated polymer can vary widely, e.g., the number of units can range from 2 to about 225, and preferably from about 5 to about 25.
• the hydrophilic polymers containing one or more thio carbonyl thio fragments of a RAFT agent can also include a unit derived from a protected monomer such as, for example, nitrogen protected monomers, acetate protected monomers, e.g., vinyl acetate, and the like.
• nitrogen protected monomers (“NPM”) have an amino group that is protected by a nitrogen protecting group.
• nitrogen protecting group means a group attached to a nitrogen atom to preclude that nitrogen atom from participating in a polymerization reaction.
• secondary amine groups can be protected in accordance with the invention, in most embodiments the protected amino group provides a primary amine group following deprotection.
• Suitable nitrogen protecting groups include, but are not limited to: (a) “carbamate-type” groups of the formula C(O)O—R′, wherein W is an aromatic or aliphatic hydrocarbon group, which may be optionally substituted and which, taken together with the nitrogen atom to which it is attached forms a carbamate group; (b) “amide-type” groups of the formula —C(O)—R′′ wherein R′′ is for example methyl, phenyl, trifluoromethyl, and the like, which taken together with the nitrogen atom to which they are attached form an amide group; (c) “N-sulfonyl” derivatives, that is groups of the formula —SO 2 —R′′′ wherein R′′′ is, for example, tolyl, phenyl, trifluoromethyl, 2,2,5,7,8-pentamethylchroman-6-yl-, 2,3,6-trimethyl-4-methoxybenzene, and the like.
• nitrogen protecting groups include, but are not limited to, benzyloxycarbonyl (CBZ), p-methoxybenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, tert-butoxycarbonyl (t-BOC), 9-flourenylmethyloxycarbonyl (Fmoc), 2-chlorobenzyloxycarbonyl, allyloxycarbonyl (alloc), 2-(4-biphenyl)propyl-2-oxycarbonyl (Bpoc), 1-adamantyloxycarbonyl, trifluoroacetyl, toluene sulphonyl and the like.
• CBZ benzyloxycarbonyl
• p-methoxybenzyloxycarbonyl p-methoxybenzyloxycarbonyl
• p-nitrobenzyloxycarbonyl tert-butoxycarbonyl
• t-BOC tert-butoxycarbonyl
• examples of t-Boc protected monomers include 2-(2-(tert-butoxycarbonylamino)acetoxy)ethyl methacrylate, 2-(2-(tert-butoxycarbonylamino)acetamido)ethyl methacrylate, 2-(tert-butoxycarbonylamino)ethyl butoxycarbonylamino)ethyl-N-vinylcarbamate, 3-(2-(tert-butoxycarbonylamino)acetoxy)-2-hydroxypropyl, N-(tert-Butoxycarbonyl)-L-glutamic acid methacryloxyethyl ester, 2-(tert-butoxycarbonylamino)-6-(3-(2-(methacryloyloxy)ethyl)ureido)hexanoic acid, 2-(tert-butoxycarbonylamino)-3-(methacryloyloxy)propanoic acid, 2-(tert-butoxycarbonyla
• the nitrogen protecting groups present in the hydrophilic polymer can be readily removed post-polymerization by well known methods in the chemical art. Techniques for protecting amino nitrogen atoms with nitrogen protecting groups, and for deprotecting amino nitrogen atoms after a particular reaction are well known in the chemical art. See, for example, Greene et al., Protective Groups in Organic Synthesis, John Wiley & Sons, 1991, and U.S. Provisional Ser. Nos. 61/113,736; 61/113,739; 61/113,742; and 61/113,746, the contents of which are incorporated by reference herein.
• an NPM can be prepared by reaction of a nitrogen-protected amino acid or amino alcohol with an ethylenically unsaturated compound having a group reactive with the respective acid or an alcohol group.
• a nitrogen protected amino acid may also have an unprotected amine group or a hydroxyl group, and the second amine group or the hydroxyl group, respectively, is the site of reaction to attach the ethylenic unsaturation. If the nitrogen protected amino acid has multiple available sites of attachment of an ethylenically unsaturated group NPM monomers having two or more ethylenically unsaturated groups may be produced.
• these monomers are usually hydrophobic in the “protected” or “blocked” form.
• the protecting group e.g., in the case of the t-Boc monomers
• the biomedical device becoming more hydrophilic in nature and the material could therefore retain more water.
• Methods for removing the protecting group are within the purview of one skilled in the art.
• the size of the hydrophilic units can vary widely, e.g., the number of units can range from 10 to about 3000, and preferably from about 50 to about 1000.
• the resulting hydrophilic polymers can be in the form of homopolymers, block copolymers and random copolymers.
• the hydrophilic polymers will have a number average molecular weight ranging from about 1,000 to about 300,000 and about 10,000 to about 100,000.
• a is from about 10 to about 2,700.
• x is from about 15 to about 3000 and y is from about 1 to about 250.
• x is from about 12 to about 3000 and y is from about 1 to about 250.
• the one or more comonomers employed in the mixtures to be polymerized to form a biomedical device of the present invention include conventional biomedical device-forming or ophthalmic lens-forming monomers.
• the term “monomer” or “monomeric” and like terms denote relatively low molecular weight compounds that are polymerizable by free radical polymerization, as well as higher molecular weight compounds also referred to as “prepolymers”, “macromonomers”, and related terms.
• the biomedical device-forming comonomer contains at least one polymerizable group.
• a suitable comonomer includes hydrophobic monomers, hydrophilic monomers and the like and mixtures thereof.
• hydrophilic comonomers include, but are not limited to, unsaturated carboxylic acids, such as methacrylic and acrylic acids; (meth)acrylic substituted alcohols or polyols such as 2-hydroxyethyl methacrylate, 2-hydroxyethyl acrylate, glyceryl methacrylate and the like; vinyl lactams such as N-vinylpyrrolidone and the like; and (meth)acrylamides such as methacrylamide, N,N-dimethylacrylamide and the like and combinations thereof. Still further examples are the hydrophilic vinyl carbonate or vinyl carbamate monomers disclosed in U.S. Pat. No.
• hydrophilic monomers can be present in the mixtures in an amount ranging from about 0.1 to about 90 weight percent, based on the total weight of the mixture.
• the initial mixture to be polymerized can comprise at least one (meth)acrylic substituted alcohol, such as at least one of 2-hydroxyethyl methacrylate and glyceryl methacrylate, preferably in an amount of at least about 0.1 to about 50 weight percent.
• the mixture to be polymerized further includes at least one vinyl lactam, such as N-vinylpyrrolidone and/or at least one (meth)acrylamide, such as N,N-dimethylacrylamide.
• Suitable hydrophobic monomers include C 1 -C 20 alkyl and C 3 -C 20 cycloalkyl (meth)acrylates, substituted and unsubstituted C 6 -C 30 aryl (meth)acrylates, (meth)acrylonitriles, fluorinated alkyl methacrylates, long-chain acrylamides such as octyl acrylamide, and the like.
• the hydrophobic monomers can be present in the mixtures in an amount ranging from about 0.1 to about 90 weight percent, based on the total weight of the mixture.
• silicone-containing monomers Another class of device-forming or lens-forming monomers is silicone-containing monomers.
• a silicone-containing comonomer which contains from 1 to about 60 silicone atoms, in addition to the hydrophilic polymer containing one or more thio carbonyl thio fragments of a RAFT agent, may be included in the initial mixture, for example, if it is desired to obtain a copolymer with high oxygen permeability.
• Applicable silicone-containing monomers for use in the formation of contact lenses such as silicone hydrogels are well known in the art and numerous examples are provided in, for example, U.S. Pat. Nos. 4,136,250; 4,153,641; 4,740,533; 5,034,461; 5,070,215; 5,260,000; 5,310,779; and 5,358,995.
• silicon-containing monomers include bulky polysiloxanylalkyl(meth)acrylic monomers.
• An example of a bulky polysiloxanylalkyl(meth)acrylic monomer is represented by the structure of Formula V:
• X denotes —O— or —NR— wherein R denotes hydrogen or a C 1 -C 4 alkyl; each R 6 independently denotes hydrogen or methyl; each R 7 independently denotes a lower alkyl radical, phenyl radical or a group represented by
• each R 7′ independently denotes a lower alkyl or phenyl radical; and h is 1 to 10.
• Representative examples of other applicable silicon-containing monomers includes, but are not limited to, bulky polysiloxanylalkyl carbamate monomers as generally depicted in Formula Va:
• X denotes —NR—; wherein R denotes hydrogen or a C 1 -C 4 alkyl; R 6 denotes hydrogen or methyl; each R 7 independently denotes a lower alkyl radical, phenyl radical or a group represented by
• each R 7′ independently denotes a lower alkyl or phenyl radical; and h is 1 to 10, and the like.
• Examples of bulky monomers are 3-methacryloyloxypropyltris(trimethyl-siloxy)silane or tris(trimethylsiloxy)silylpropyl methacrylate, sometimes referred to as TRIS and tris(trimethylsiloxy)silylpropyl vinyl carbamate, sometimes referred to as TRIS-VC and the like and mixtures thereof.
• Such bulky monomers may be copolymerized with a silicone macromonomer, which is a poly(organosiloxane) capped with an unsaturated group at two or more ends of the molecule.
• a silicone macromonomer which is a poly(organosiloxane) capped with an unsaturated group at two or more ends of the molecule.
• U.S. Pat. No. 4,153,641 discloses, for example, various unsaturated groups such as acryloxy or methacryloxy groups.
• silicone-containing monomers includes, but is not limited to, silicone-containing vinyl carbonate or vinyl carbamate monomers such as, for example, 1,3-bis[4-vinyloxycarbonyloxy)but-1-yl]tetramethyldisiloxane; 3-(trimethylsilyl)propyl vinyl carbonate; 3-(vinyloxycarbonylthio)propyl-[tris(trimethylsiloxy)silane]; 3-[tris(trimethylsiloxy)silyl]propyl vinyl carbamate; 3-[tris(trimethylsiloxy)silyl]propyl allyl carbamate; 3-[tris(trimethylsiloxy)silyl]propyl vinyl carbonate; t-butyldimethylsiloxyethyl vinyl carbonate; trimethylsilylethyl vinyl carbonate; trimethylsilylmethyl vinyl carbonate and the like.
• silicone-containing vinyl carbonate or vinyl carbamate monomers such as, for example, 1,3-bis[4-
• silicon-containing monomers includes polyurethane-polysiloxane macromonomers (also sometimes referred to as prepolymers), which may have hard-soft-hard blocks like traditional urethane elastomers.
• silicone urethanes are disclosed in a variety or publications, including Lai, Yu-Chin, “The Role of Bulky Polysiloxanylalkyl Methacrylates in Polyurethane-Polysiloxane Hydrogels,” Journal of Applied Polymer Science, Vol. 60, 1193-1199 (1996).
• PCT Published Application No. WO 96/31792 also discloses examples of such monomers, the contents of which are hereby incorporated by reference in its entirety.
• Further examples of silicone urethane monomers are represented by Formulae VI and VII:
• D denotes an alkyl diradical, an alkyl cycloalkyl diradical, a cycloalkyl diradical, an aryl diradical or an alkylaryl diradical having 6 to about 30 carbon atoms;
• G denotes an alkyl diradical, a cycloalkyl diradical, an alkyl cycloalkyl diradical, an aryl diradical or an alkylaryl diradical having 1 to about 40 carbon atoms and which may contain ether, thio or amine linkages in the main chain;
• a is at least 1;
• A denotes a divalent polymeric radical of Formula VIII:
• each R s independently denotes an alkyl or fluoro-substituted alkyl group having 1 to about 10 carbon atoms which may contain ether linkages between the carbon atoms; m′ is at least 1; and p is a number that provides a moiety weight of about 400 to about 10,000;
• each of E and E′ independently denotes a polymerizable unsaturated organic radical represented by Formula IX:
• R 8 is hydrogen or methyl
• R 9 is independently hydrogen, an alkyl radical having 1 to 6 carbon atoms, or a —CO—Y—R 11 radical wherein Y is —O—, —S— or —NH—
• R 10 is a divalent alkylene radical having 1 to about 10 carbon atoms
• R′′ is a alkyl radical having 1 to about 12 carbon atoms
• X denotes —CO— or —OCO—
• Z denotes —O— or —NH—
• Ar denotes an aromatic radical having about 6 to about 30 carbon atoms
• w is 0 to 6
• x is 0 or 1
• y is 0 or 1
• z is 0 or 1.
• a preferred silicone-containing urethane monomer is represented by Formula X:
• m is at least 1 and is preferably 3 or 4
• a is at least 1 and preferably is 1
• p is a number which provides a moiety weight of about 400 to about 10,000 and is preferably at least about 30
• R 12 is a diradical of a diisocyanate after removal of the isocyanate group, such as the diradical of isophorone diisocyanate
• each E′′ is a group represented by:
• silicone-containing monomers includes fluorinated monomers. Such monomers have been used in the formation of fluorosilicone hydrogels to reduce the accumulation of deposits on contact lenses made therefrom, as described in, for example, U.S. Pat. Nos. 4,954,587; 5,010,141 and 5,079,319.
• silicone-containing monomers having certain fluorinated side groups, i.e., —(CF/)—H have been found to improve compatibility between the hydrophilic and silicone-containing monomeric units, see, e.g., U.S. Pat. Nos. 5,321,108 and 5,387,662.
• a biomedical device-forming comonomer can be a cationic monomer such as cationic silicone-containing monomer or cationic fluorinated silicone-containing monomers.
• the mixtures to be polymerized may include the silicone comonomer, in addition to the subject multi-armed macromonomers, at 0 to about 50 weight percent, preferably about 5 to about 30 weight percent when present.
• the mixtures to be polymerized can also include a crosslinking monomer (a crosslinking monomer being defined as a monomer having multiple polymerizable functionalities).
• a crosslinking monomer being defined as a monomer having multiple polymerizable functionalities.
• Representative crosslinking monomers include: divinylbenzene, allyl methacrylate, ethyleneglycol dimethacrylate, tetraethyleneglycol dimethacrylate, polyethyleneglycol dimethacrylate, vinyl carbonate derivatives of the glycol dimethacrylates, and methacryloxyethyl vinylcarbonate.
• this monomeric material may be included in the monomer mixture at about 0.1 to about 20 weight percent, and more preferably at about 0.2 to about 10 weight percent.
• homopolymers or copolymers within the scope of the present invention may optionally have one or more strengthening agents added prior to polymerization, preferably in quantities of less than about 80 weight percent and preferably from about 20 to about 60 weight percent.
• suitable strengthening agents are described in U.S. Pat. Nos. 4,327,203; 4,355,147; and 5,270,418; each of which is incorporated herein in its entirety by reference.
• Specific examples, not intended to be limiting, of such strengthening agents include cycloalkyl acrylates and methacrylates; e.g., tert-butylcyclohexyl methacrylate and isopropylcyclopentyl acrylate.
• the mixtures to be polymerized may further contain, as necessary and within limits not to impair the purpose and effect of the present invention, various additives such as an antioxidant, coloring agent, ultraviolet absorber, lubricant internal wetting agents, toughening agents and the like and other constituents as is well known in the art.
• various additives such as an antioxidant, coloring agent, ultraviolet absorber, lubricant internal wetting agents, toughening agents and the like and other constituents as is well known in the art.
• the biomedical devices of the present invention can be prepared by polymerizing the foregoing mixtures to form a product that can be subsequently formed into the appropriate shape by, for example, lathing, injection molding, compression molding, cutting and the like.
• the initial mixture may be polymerized in tubes to provide rod-shaped articles, which are then cut into buttons. The buttons may then be lathed into contact lenses.
• the biomedical devices such as contact lenses may be cast directly in molds, e.g., polypropylene molds, from the mixtures, e.g., by spincasting and static casting methods.
• Spincasting methods are disclosed in U.S. Pat. Nos. 3,408,429 and 3,660,545, and static casting methods are disclosed in U.S. Pat. Nos. 4,113,224, 4,197,266, and 5,271,875.
• Spincasting methods involve charging the mixture mixtures to be polymerized to a mold, and spinning the mold in a controlled manner while exposing the mixture to a radiation source such as UV light.
• Static casting methods involve charging the monomeric mixture between two mold sections, one mold section shaped to form the anterior lens surface and the other mold section shaped to form the posterior lens surface, and curing the mixture while retained in the mold assembly to form a lens, for example, by free radical polymerization of the mixture.
• free radical reaction techniques to cure the lens material include thermal radiation, infrared radiation, electron beam radiation, gamma radiation, ultraviolet (UV) radiation, and the like; or combinations of such techniques may be used.
• U.S. Pat. No. 5,271,875 describes a static cast molding method that permits molding of a finished lens in a mold cavity defined by a posterior mold and an anterior mold. As an additional method, U.S. Pat. No.
• 4,555,732 discloses a process where an excess of a monomeric mixture is cured by spincasting in a mold to form a shaped article having an anterior lens surface and a relatively large thickness, and the posterior surface of the cured spincast article is subsequently lathed to provide a contact lens having the desired thickness and posterior lens surface.
• Polymerization may be facilitated by exposing the mixture to heat and/or radiation, such as ultraviolet light, visible light, or high energy radiation.
• a polymerization initiator may be included in the mixture to facilitate the polymerization step.
• free radical thermal polymerization initiators include organic peroxides such as acetyl peroxide, lauroyl peroxide, decanoyl peroxide, stearoyl peroxide, benzoyl peroxide, tertiarylbutyl peroxypivalate, peroxydicarbonate, and the like.
• UV initiators are those known in the art and include benzoin methyl ether, benzoin ethyl ether, Darocure® 1173, 1164, 2273, 1116, 2959, 3331 (EM Industries) and Irgacure® 651 and 184 (Ciba-Geigy), and the like. Generally, the initiator will be employed in the monomeric mixture at a concentration of about 0.01 to about 5 percent by weight of the total mixture.
• Polymerization is generally performed in a reaction medium, such as, for example, a solution or dispersion using a solvent, e.g., water or an alkanol containing from 1 to 4 carbon atoms such as methanol, ethanol or propan-2-ol. Alternatively, a mixture of any of the above solvents may be used.
• a solvent e.g., water or an alkanol containing from 1 to 4 carbon atoms such as methanol, ethanol or propan-2-ol.
• a mixture of any of the above solvents may be used.
• polymerization can be carried out for about 15 minutes to about 72 hours, and under an inert atmosphere of, for example, nitrogen or argon. If desired, the resulting polymerization product can be dried under vacuum, e.g., for about 5 to about 72 hours or left in an aqueous solution prior to use.
• the mixture will contain the hydrophilic polymer comprising one or more hydrophilic units and one or more thio carbonyl thio fragments of a RAFT agent in an amount ranging from about 0.25 to about 15 weight percent, and preferably about 2.5 to about 7.5 weight percent, based on the total weight of the mixture.
• the biomedical device-forming comonomer may be present in the mixture in an amount ranging from about 70 to about 99 weight percent, and preferably from about 80 to about 95 weight percent, based on the total weight of the mixture.
• the mixture may further include at least a diluent that is ultimately replaced with water when the polymerization product is hydrated to form a hydrogel.
• the water content of the hydrogel is greater than about 5 weight percent and more commonly between about 10 to about 80 weight percent.
• the amount of diluent used should be less than about 50 weight percent and in most cases, the diluent content will be less than about 30 weight percent.
• the actual limit will be dictated by the solubility of the various monomers in the diluent.
• Suitable diluents include, but are not limited to, ethylene glycol; glycerine; liquid poly(ethylene glycol); alcohols; alcohol/water mixtures; ethylene oxide/propylene oxide block copolymers; low molecular weight linear poly(2-hydroxyethyl methacrylate); glycol esters of lactic acid; formamides; ketones; dialkylsulfoxides; butyl carbitol; and the like and mixtures thereof.
• the mixture used to produce the hydrogel lens may further include crosslinking and wetting agents known in the prior art for making hydrogel materials.
• the mixtures to be polymerized may further include a monomer for increasing the refractive index of the resultant copolymer.
• a monomer for increasing the refractive index of the resultant copolymer examples include aromatic (meth)acrylates, such as phenyl(meth)acrylate, 2-phenylethyl(meth)acrylate, 2-phenoxyethyl methacrylate, and benzyl(meth)acrylate.
• the biomedical devices such as contact lenses obtained herein may be subjected to optional machining operations.
• the optional machining steps may include buffing or polishing a lens edge and/or surface.
• machining processes may be performed before or after the product is released from a mold part, e.g., the lens is dry released from the mold by employing vacuum tweezers to lift the lens from the mold, after which the lens is transferred by means of mechanical tweezers to a second set of vacuum tweezers and placed against a rotating surface to smooth the surface or edges. The lens may then be turned over in order to machine the other side of the lens.
• the lens may then be transferred to individual lens packages containing a buffered saline solution.
• the saline solution may be added to the package either before or after transfer of the lens.
• Appropriate packaging designs and materials are known in the art.
• a plastic package is releasably sealed with a film. Suitable sealing films are known in the art and include foils, polymer films and mixtures thereof.
• the sealed packages containing the lenses are then sterilized to ensure a sterile product. Suitable sterilization means and conditions are known in the art and include, for example, autoclaving.
• Such other steps can include, for example, coating the formed lens, surface treating the lens during formation (e.g., via mold transfer), inspecting the lens, discarding defective lenses, cleaning the mold halves, reusing the mold halves, and the like and combinations thereof.
• NVP N-vinyl-2-pyrrolidone
• TRIS-MA tris(trimethylsiloxy)silylpropyl methacrylate
• TRIS-VC tris(trimethylsiloxy)silylpropyl vinyl carbamate
• VazoTM 64 azo bis-isobutylnitrile (AIBN)
• Vinal Acid Vinylcarbamate of 13-Alanine having the structure:
• V2D25 Divinylcarbonate of PDMS diol having the structure:
• Ma2D37 Dimethacrylamide of a PDMS diamine having the structure:
• CIX-4 a compound having the structure:
• TEGDMA a compound having the structure:
• M1-MCR-C12 a compound having the structure:
• n is an average of 12.
• a 500 mL round bottom 3 neck flask was fitted with a magnetic stirrer, nitrogen inlet, and a temperature probe.
• Ethyl-2-bromo propionate (27.2 g) and 500 mL absolute ethanol were combined and stirred for 20 minutes under nitrogen.
• the reaction flask was placed in an ice/water bath at 0° C.
• Potassium O-ethyl xanthate (26.4 g) was slowly added using a powder funnel
• the funnel was rinsed with an additional 50 mL of ethanol.
• the reaction flask was allowed to stir for an additional 24 hours at room temperature.
• Deionized water 250 mL was then added to the reaction flask.
• a 250 mL round bottom 3 neck flask was fitted with a magnetic stirrer, nitrogen inlet, Freidrich's condenser, and a temperature probe. After absolute ethanol (125 mL) and benzyl bromide (14.4 g) were added, the reaction flask was placed in an ice/water bath at 0° C. and stirred for 1 hour. Potassium O-ethyl xanthate (17.63 g) was added slowly to the reaction flask using a powder funnel. The reaction flask was stirred for an additional 16 hours at room temperature and 200 mL of purified water was added to the flask.
• a 500 mL round bottom 3 neck flask was fitted with a magnetic stirrer, nitrogen inlet, and a temperature probe, 1-bromoethyl benzene (20.5 mL) and 200 mL absolute ethanol were added.
• the reaction flask was placed in an ice/water bath at 0° C. Potassium O-ethyl xanthate was added slowly using a powder funnel rinsed into the reaction flask with an additional 100 mL ethanol.
• the reaction flask was allowed to stir for an additional 24 hours at room temperature and then 250 mL of purified water was added.
• the crude mixture was extracted 4 times with 200 mL of 2:1 heptane:ethyl ether retaining the organic layers.
• Hydrophilic Polymers (Macroraft Reagents).
• the Hydrophilic Polymers of Examples 6-27 were prepared in substantially the same manner as in Example 5.
• the ingredients and amounts for preparing the hydrophilic polymers are set forth below in Table 1.
• a reaction flask was fitted a magnetic stirrer, ice bath, dropping funnel and a nitrogen inlet.
• the flask was charged with ethyl ether (150 ml) and 60% sodium hydride (6.3 grams).
• dodecylmercaptan (30.76 grams) was slowly added to the cold slurry (temperature 5-10° C.).
• the grayish slurry was converted to a thick white slurry (sodium thiodecylate) with vigorous evolution of H2 gas.
• the mixture was cooled to 0° C. and carbon disulfide (12 g) was added.
• a 500 mL round bottom 3 neck flask was equipped with a Friedrich condenser, a magnetic stirring bar, nitrogen inlet, and a temperature probe. Ethyl-2-bromo propionate and 500 mL absolute ethanol were added and stirred for 20 minutes under nitrogen.
• the reaction flask was placed in an ice bath at 0° ⁇ 3° C. Potassium O-ethyl xanthate was added slowly to the reaction flask using a powder funnel and rinsed with an additional 50 mL of ethanol.
• the reaction flask was allowed to stir and equilibrate to room temperature over a period of 24 hours. DI water (250 mL) was added to quench the reaction.
• the crude mixture was extracted 4 times with 200 mL of 2:1 hexane:ethyl ether retaining the organic layers. The combined organic layers were dried over sodium sulfate, filtered and solvent was removed under reduced pressure.
• a 500 mL round bottom 3 neck flask was equipped with a magnetic stirrer, nitrogen inlet, Friedrich's condenser and a temperature probe. Ethyl (2-bromo-2-phenyl)acetate and 250 mL absolute ethanol were added and stirred for 20 minutes under nitrogen. The reaction flask was placed in an ice/water bath at 0° C. Potassium O-ethyl xanthate was added slowly using a powder funnel and rinsed into the reaction flask with an additional 50 mL of ethanol. The reaction flask was allowed to stir for an additional 24 hours at room temperature. DI water (250 mL) was then added to the reaction flask. The crude mixture was extracted 4 times with 200 mL of 2:1 hexane:ethyl ether retaining the organic layers. The combined organic layers were dried over sodium sulfate, filtered and solvent was removed under reduced pressure. Yield, 96%.
• a 250 mL round bottom 3 neck flask was equipped with a mechanical stirrer, Friedrich's condenser and a temperature probe. Carbon disulfide and dodecanethiol were added to the flask with 65 mL chloroform. Triethylamine was added drop wise using an addition funnel with 10 mL chloroform. The reaction stirred for 3 hours at room temperature. Ethyl- ⁇ -bromo proprionate was added drop wise using an addition funnel with 25 mL chloroform. The reaction flask was allowed to stir for an additional 24 hrs at room temperature. The crude mixture was washed 2 times each with 250 mL of DI water, 5% HCl, and 5% Brine retaining the organic layers. The organic layers were dried over magnesium sulfate, filtered and solvent was removed under pressure. The product was further purified by column chromatography on silica gel using hexane:ethyl acetate.
• a 250 mL round bottom 3 neck flask was equipped with a mechanical stirrer, Friedrich condenser and a temperature probe. Carbon disulfide and dodecanethiol were added to the flask with 65 mL chloroform. Triethylamine was added dropwise using an addition funnel with 10 mL chloroform. The reaction stirred for 3 hours at room temperature. Ethyl- ⁇ -bromophenyl acetate was added drop wise using an addition funnel with 35 mL chloroform. The reaction flask was allowed to stir for an additional 24 hours at room temperature. The crude mixture was washed 2 times with 250 mL of DI water, 5% HCl (aq), and 5% Brine retaining the organic layers. The organic layers were dried over magnesium sulfate, filtered and solvent was removed under pressure. The product was further purified by column chromatography on silica gel using hexane:ethyl acetate.
• the resulting hydrophilic polymer was isolated by precipitation into a large volume (3 L) of ethyl ether.
• the isolated yield of polymer was 21.6 grams (37%).
• the resulting hydrophilic polymer was isolated by precipitation into a large volume of ethyl ether.
• the isolated yield of the hydrophilic polymer was 6.05 grams (29%).
• the resulting hydrophilic polymer was isolated by precipitation into a large volume of ethyl ether.
• the isolated yield of the hydrophilic polymer was 45.34 grams.
• Contact lenses, films and lens flats were prepared in polypropylene molds. Flat thicknesses of 300, 450, 550 and 650 ⁇ m were cast in order to obtain the oxygen permeability of the materials. Lens samples were cast to determine water content, modulus, tensile strength, percent elongation and tear strength.
• Films were cast between 3.5 ⁇ 4 inch silane treated glass plates separated by Teflon gaskets ranging from 0.2 to 1 mm in thickness. Films were cured under UV light at 55° C. or ambient temperature for 1-2 hours. Films were extracted by swelling in 100% isopropyl alcohol for four hours. The isopropyl alcohol concentration was reduced to 50% with water and then samples were stepped into 100% water. Film samples were used for mechanical testing and water content measurements.
• Water % Two sets of six hydrated lenses or films are blotted dry on a piece of filter paper to remove excess water, and samples are weighed (wet weight). Samples are then placed in a microwave oven for 10 minutes inside a jar containing dessicant. The samples are then allowed to sit for 30 minutes to equilibrate to room temperature and reweighed (dry weight). The percent water is calculated from the wet and dry weights.
• Modulus and elongation tests were conducted according to ASTM D-1708a, employing an Instron (Model 4502) instrument where the hydrogel film sample is immersed in borate buffered saline; an appropriate size of the film sample is gauge length 22 mm and width 4.75 mm, where the sample further has ends forming a dogbone shape to accommodate gripping of the sample with clamps of the Instron instrument. All results are based on the average thickness at the center. The standard deviation is given in parenthesis.
• Oxygen permeability Dk was determined by the following procedure. Other methods and/or instruments may be used as long as the oxygen permeability values obtained therefrom are equivalent to the described method.
• the oxygen permeability of silicone hydrogels is measured by the polarographic method (ANSI Z80.20-1998) using an O 2 Permeometer Model 201T instrument (Createch, Albany, California USA) having a probe containing a central, circular gold cathode at its end and a silver anode insulated from the cathode. Measurements are taken only on pre-inspected pinhole-free, flat silicone hydrogel film samples of four different center thicknesses ranging from 150 to 600 microns. Center thickness measurements of the film samples may be measured using a Rehder ET-1 electronic thickness gauge.
• the film samples have the shape of a circular disk. Measurements are taken with the film sample and probe immersed in a bath containing circulating phosphate buffered saline (PBS) equilibrated at 35° C.+/ ⁇ 0.2°. Prior to immersing the probe and film sample in the PBS bath, the film sample is placed and centered on the cathode premoistened with the equilibrated PBS, ensuring no air bubbles or excess PBS exists between the cathode and the film sample, and the film sample is then secured to the probe with a mounting cap, with the cathode portion of the probe contacting only the film sample.
• PBS circulating phosphate buffered saline
• Teflon polymer membrane e.g., having a circular disk shape
• the Teflon membrane is first placed on the pre-moistened cathode, and then the film sample is placed on the Teflon membrane, ensuring no air bubbles or excess PBS exists beneath the Teflon membrane or film sample.
• Example 53 into a one neck, 250 mL round bottom flask equipped with a magnetic stirring bar was added 392 mg (0.891 mmol) of ethyl ⁇ -dodecyltrithiocarbonyl phenyl acetate (EDTCPA), 43 mL of DMA (41.4 g, 0.4173 moles), 4.629 g of monomethoxy polyethylene glycol 1000 methacrylate (mPEG) (4.21 mmol) and 100 mL of anhydrous 1,4-dioxane. After these components were thoroughly mixed, one mL of an 8.59 mM AIBN solution in 1,4-dioxane (1.41 mg/mL) was then carefully pipetted into the flask.
• EDTCPA ethyl ⁇ -dodecyltrithiocarbonyl phenyl acetate
• DMA 41.4 g, 0.4173 moles
• mPEG monomethoxy polyethylene glycol 1000 methacrylate
• the round bottom flask was closed with an appropriately sized rubber septum and the contents of the flask were then purged by bubbling dry nitrogen gas for 1 hour.
• the contents of the reaction flask were heated to 60° C. with an oil bath for 18 hours, cooled to room temperature, and precipitated dropwise into 2500 mL of ether while stirring vigorously.
• the polymer product was then filtered and dried under vacuum to remove residual ether.
• Examples 54 through 58 were carried out in the same manner as Example 53 except using varying amounts of mPEG and DMA and the type of mPEG.
• the RAFT agent utilized in each of the examples was EDTCPA in approximately 0.390 g for each example.
• the amounts of the ingredients are set forth below in Table 4.
• Lens flats were cast in order to obtain the oxygen permeability of the materials. Contact lenses were cast to determine water content, modulus, tensile strength, percent elongation and tear strength.
• Tribological testing was performed on a CETR Model UMT-2 micro-tribometer. Each lens was clamped on an HDPE holder that initially mates with the posterior side of the lens. A poly(propylene) clamping ring was then used to hold the edge region of the lens. Once the lens was mounted in the holder the assembly was placed in a stationary clamping device within the micro-tribometer. A polished stainless steel disc containing 1 mL of phosphate buffered saline (PBS) was then brought into contact with the lens and F N was adjusted to 2 grams over the course of the run for the frictional measurements.
• PBS phosphate buffered saline
• the stainless steel disc was rotated at a velocity of 12 cm/sec for a duration of 20 seconds in both the forward and reverse directions and the peak (static) and average (kinetic) COF values were recorded. Each value represents the average of 6 lenses. All data was normalized to the average values obtained at 2 g force from the lens holder in the absence of a lens tested in PBS. PBS was used as the test-in solution for every lens.
• Captive Bubble Contact Angle Captive bubble contact angle data was collected on a First Ten Angstroms FTA-1000 prop Shape Instrument. All samples were rinsed in HPLC grade water prior to analysis in order to remove components of the packaging solution from the sample surface. Prior to data collection the surface tension of the water used for all experiments was measured using the pendant drop method. In order for the water to qualify as appropriate for use, a surface tension value of 70-72 dynes/cm was expected. All lens samples were placed onto a curved sample holder and submerged into a quartz cell filled with HPLC grade water. Advancing and receding captive bubble contact angles were collected for each sample. The advancing contact angle is defined as the angle measured in water as the air bubble is retracting from the lens surface (water is advancing across the surface).
• the contact angle was calculated at the digital frame just prior to contact line movement across the sample/air bubble interface.
• the receding contact angle is defined as the angle measured in water as the air bubble is expanding across the sample surface (water is receding from the surface).
• AIBN was added to a 500 mL round bottom flask equipped with a magnetic stirring bar.
• ethyl- ⁇ -(O-ethylxanthyl) propionate (EEXP), 1,4-dioxane, and NVP were added to the flask.
• the flask was then sealed with a rubber septum and purged with N 2 for 30 minutes.
• the flask was placed in an oil bath (60° C.) for 16 hours. After cooling to room temperature, the contents of the flask were precipitated into 4 L of diethyl ether. The precipitate was isolated by filtration and dried in vacuo to provide the PVP MacroRAFT agent.
• the amount of the ingredients for each of Examples 62 and 63 are set forth below in Table 8.
• Examples 65 and 66 were carried out in substantially the same manner using the hydrophilic polymer from Examples 60 and 61, respectively.
• Example 68 was carried out in substantially the same manner using the hydrophilic polymer from Example 63.
• Formulations were prepared in which 0.3 g of the uncleaved hydrophilic polymers from Examples 59-63 and the cleaved hydrophilic polymers of Comparative Examples F-J were dissolved in 1.7 g of the mixture obtained in Comparative Example A (see Table 2). Films of all of these formulations were cast between glass plates and cured in the UV oven for 2 hours. Films were removed from glass slides and placed in the vacuum oven at 80° C. for 2 hours and at room temperature. Films were cut into pieces for percent extractables and % water determination. For percent extractables, films were weighed, extracted in 20 mL of isopropyl alcohol overnight, decanted off the isopropyl alcohol and dried sample in a vacuum oven before reweighing. For % water, additional samples were extracted in isopropyl alcohol overnight and then exchanged with deinonized water several times before being weighed in its hydrated state, dried in the vacuum oven and reweighed. Results for this study are set forth below in Table 9.
• the higher percent extractables can also be explained by the end group (trithiocarbonate or xanthate) slowing the polymerization of the network down (confirmed by DSC measurements) and leading to higher residual monomer left at the end of the polymerization.
• This example shows the advantageous effect of having the thio carbonyl thio group on the polymer during the polymerization.

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